|
HS Code |
281742 |
| Chemical Name | 2,6-Pyridinecarboxylic acid |
| Other Names | Dipicolinic acid |
| Molecular Formula | C7H5NO4 |
| Molar Mass | 167.12 g/mol |
| Appearance | White crystalline solid |
| Melting Point | 247-250 °C |
| Solubility In Water | Moderate |
| Density | 1.573 g/cm3 |
| Cas Number | 98-98-6 |
As an accredited 2.6-pyridine carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2,6-pyridine dicarboxylic acid is packaged in a sealed amber glass bottle with a detailed hazard and handling label. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2,6-pyridine carboxylic acid: Typically loaded in 25 kg bags, totaling approximately 16–18 metric tons per container. |
| Shipping | **Shipping Description for 2,6-Pyridine Dicarboxylic Acid:** Ship in tightly sealed, corrosion-resistant containers. Store in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials. Follow all relevant transportation regulations for chemicals. Label packaging clearly with hazard warnings and ensure proper documentation accompanies the shipment. Handle with appropriate protective equipment. |
| Storage | 2,6-Pyridine dicarboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances, such as strong oxidizing agents. Protect from moisture and direct sunlight. Use non-sparking tools when handling. Label the storage container clearly, and keep it out of reach of unauthorized personnel. |
| Shelf Life | 2,6-Pyridine carboxylic acid typically has a shelf life of 2-3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 2.6-pyridine carboxylic acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular weight 123.11 g/mol: 2.6-pyridine carboxylic acid with a molecular weight of 123.11 g/mol is used in agrochemical manufacturing, where it enables precise stoichiometric calculations. Melting point 164°C: 2.6-pyridine carboxylic acid with a melting point of 164°C is used in organic reaction processes, where it provides thermal stability during high-temperature operations. Particle size <50 µm: 2.6-pyridine carboxylic acid with particle size less than 50 µm is used in catalyst formulation, where it allows improved dispersion and reactivity. Stability temperature up to 120°C: 2.6-pyridine carboxylic acid with stability temperature up to 120°C is used in specialty coatings, where it maintains chemical integrity under moderate heat exposure. |
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There is a whole world of chemicals out there, and 2.6-pyridine carboxylic acid has carved out its place among them. Plenty of researchers, production specialists, and industrial chemists keep it close because of its versatility and the reliability it brings to complex reactions. Its molecular structure, featuring two carboxylic acid groups on a pyridine ring, lets it play a unique role that you just don't get from straightforward benzoic acid or single-substituted pyridine derivatives.
Chemistry doesn't always need bells and whistles. There is real satisfaction in materials that do what they promise every time. 2.6-pyridine carboxylic acid stands out because it's structurally simple yet functionally rich. Holding a molecular formula of C7H5NO4, and also called dipicolinic acid, this compound has become a mainstay in many laboratories. Its melting point sits high enough to prevent problems in standard shipping and storage. It dissolves well in water and polar solvents, which makes it easy to work with during reaction planning. These features offer reliability, especially if you're dealing with water-based synthesis or need solid-state stability.
Life in the lab teaches you the importance of clean reactions. 2.6-pyridine carboxylic acid enters the scene in bacterial spore research—one of its key claims to fame. It shows up as a natural component of some bacterial spores, giving the spores extra resilience by forming chelates with calcium ions. This characteristic lets microbiologists and biochemists use it as a marker for hard-to-kill spores in sterilization studies. In my time researching sterilization, I've seen how its presence can swing the results of viability testing. Pharmaceutical companies note its role as part of the spore’s resistance to heat and radiation, which drives their choice to use purified standards of 2.6-pyridine carboxylic acid in process testing and validation.
Diving into organic synthesis, its chelating ability means it forms tight complexes with a wide range of metal ions. Coordinating transition metals or rare earths, for example, gives researchers room to design selective catalysts and separation agents. This isn't some far-fetched application—mainstream analysts and synthetic chemists rely on this attribute for everything from environmental clean-up to building new kinds of ligands.
There’s more: 2.6-pyridine carboxylic acid facilitates research into supramolecular assemblies—structures larger than a single molecule but formed through subtle non-covalent forces. Here, its ability to act as a bridge between other molecules becomes invaluable. Scientists benefit when they try to tune properties like solubility, magnetic response, or charge transfer in new materials. In teaching labs, this compound’s reliable behavior supports demonstration experiments in undergraduate courses, emphasizing metal-ligand chemistry without headaches from unreliable results.
Anyone who has compared it with isomers like 2.4-pyridine carboxylic acid or the well-known nicotinic acid (vitamin B3) can quickly spot the differences. Position matters. The two carboxyl groups on the 2 and 6 positions of the ring change how the molecule coordinates metals, holds on to protons, and reacts with bases and acids. It doesn’t show the nutritional value or pharmacology of nicotinic acid, so there is no confusion with food or supplement chemistry.
As an example from my own project files, using isonicotinic acid gave less selective outcomes in metal complexation trials, while 2.6-pyridine carboxylic acid yielded defined, predictable complexes. This tracks with published work showing improved crystallinity and spectral clarity using the 2.6-compound. The layout of carboxylic acids within the ring promotes both stability and distinctiveness, especially when purifying target complexes or running analytic separations. Some chemists reach for phthalic acid or standard benzoic acid, but those lack the nitrogen and separation of acid groups that drive the chelation phenomenon seen with 2.6-pyridine carboxylic acid.
Nobody working with precise reactions likes taking chances with off-spec ingredients. Purity affects everything. Technical grade material can carry trace elements or leftover solvent that force unwanted side reactions or cloud analysis. Analytical chemistry—and by extension, pharmaceutical reliability—demands consistently clean material. Labs trust sources with documented purity and verified absence of key contaminants, usually confirming identity with infrared spectroscopy or melting point checks.
High-purity 2.6-pyridine carboxylic acid opens the door for medical research and trace analysis work. The less uncertainty in your base reagents, the more dependable your conclusions. Studying spore detection tools or calibrating metal chelation tests, I found lab time was never wasted chasing odd results traced back to subpar chemicals, and 2.6-pyridine carboxylic acid has become a straightforward choice in these settings.
Making the leap from bench scale to industrial processes brings new challenges that the product is ready to face. Process chemists in bulk pharmaceutical manufacturing or fine chemical production see its value in predictable behavior and scalable synthesis. There’s no guesswork about decomposition or mishaps at scale, because its robust structure lets it hold up through heating, solvent changes, and purification cycles.
Industries that need high selectivity in extraction methods for rare earths or transition metals often use the 2.6 variant for exactly this reason. It can draw a line between closely related elements during separation, which cuts waste and increases efficiency. I’ve seen how a well-designed chelation phase can reduce both time and cost in an extraction process, and few other affordable building blocks match this performance.
Talk about innovation often starts with finding the right base chemical. Many new materials, such as coordination polymers, luminescent complexes, and advanced magnetic materials, build on ligands that lock in place—2.6-pyridine carboxylic acid does just that. Materials scientists use it to steer the assembly of intricate frameworks that underpin improved battery technology, smart sensors, and selective adsorbents.
Its molecular geometry encourages orderly packing and defined bonding with transition metals. Comparing it with other dicarboxylic acids or simple pyridine rings, researchers report sharper spectral signals and cleaner phase transitions—valuable traits in exploring solid-state properties and long-term stability. From practical experience, lab teams value this combination of effectiveness and accessibility because it bridges the gap between academic theory and pilot-scale production.
Concerns about the impact of industrial chemicals make safety practices and environmental impact especially important. 2.6-pyridine carboxylic acid brings certain advantages—its relatively low volatility and its stability cut risks of accidental vapor exposure or unexpected reactivity. The main issue comes from its acidity and reactivity with strong oxidizers. Lab teams wear gloves and lab coats and ensure good airflow when weighing and transferring. In waste handling, its solubility makes neutralization followed by controlled disposal practical for routine procedures. Recognizing these properties, many universities include it on the list of ‘sensible’ reagents for upper-level lab instruction. I’ve seen it ease the burden on chemical safety training, as new students can handle its risks with basic protocols.
Its use in spore detection also intersected with broader goals around sterilization and infection control, areas with huge impact for public health systems. The reliability of its chemical signals links directly to the success of sterilization processes—cutting the risk of incomplete sterilization in hospitals, public health labs, and food safety inspections.
Lab professionals appreciate reagents that ship safely and store easily. The solid form of 2.6-pyridine carboxylic acid handles standard transit conditions without incident, unlike compounds with high moisture sensitivity or dangerous volatility. Manufacturers package it in sealed glass or high-density plastic containers, and there’s no special refrigeration required for ordinary lab work. In my own group, we’ve stored it alongside other acids and base-sensitive reagents, knowing it resists decomposition under typical shelf conditions and doesn’t exude troubling fumes or corrosive vapors.
Because it doesn’t present the merchandising headaches of controlled substances, bulk order and restock cycles don’t create delays or regulatory hurdles in most areas. Some care goes into protection from direct sunlight and humidity, but good packaging solves these problems. This reliability cuts down the chance for unexpected lab downtime and wasted batches, an everyday concern in teaching, R&D, and production settings alike.
None of this matters if you can’t get what you need when demand spikes. 2.6-pyridine carboxylic acid is widely produced, thanks in part to its value in spore chemistry and metal separation work. Suppliers keep stable inventories, and most synthetic routes use feedstocks that parallel those for commodity pyridine—this keeps prices reasonable and supply disruptions rare.
The sustainability question doesn’t get ignored. Process improvements in the past decade have reduced byproducts and solvent waste, particularly by using continuous-flow reactors and catalytic oxidation over older batch methods. I’ve watched as improvements in product isolation and washing have been adopted to cut down water and energy use, reflecting both industry pressure and regulatory oversight. Ongoing research into greener synthesis and better waste reclamation shows optimism for making production even less resource-intensive, all without undercutting the product’s reliability or quality.
Consistency is a quiet strength in any chemical—one that 2.6-pyridine carboxylic acid supplies in spades. My work with university and private sector research teams always comes back to the need for repeatable outcomes. Research labs want to avoid wasting weeks tracing errors back to unpredictable materials. The reassurance that this acid offers—clean melting point, stable storage, high recovery after recrystallization—can’t be understated.
Some applications ride on minute details, like the sharpness of NMR spectra or the repeatability of metal binding constants. Who wants surprise artifacts or lingering contamination? It's easy to overlook the importance of smooth supply until you need it yourself. Using 2.6-pyridine carboxylic acid, researchers in analytical, environmental, and materials chemistry share similar stories—results stay reliable, and the path from hypothesis to publication gets smoother.
Even with all its advantages, 2.6-pyridine carboxylic acid can present hurdles. Large-scale buyers in developing economies sometimes face inconsistent quality or slow shipping, especially through third-party vendors. Spot checks for identity and purity become critical, especially if regulators expect traceability on every batch. Local synthesis can ease this burden, but not every region has the capacity or infrastructure to match quality guarantees set by bigger players. Agencies and buyers now set higher standards, requiring rigorous paperwork and test data for each shipment, which adds time and cost to each transaction.
Safety and environmental concerns from waste handling remain modest compared to legacy chemicals, but the need for sound neutralization and disposal hasn't disappeared. Shortcomings in documentation sometimes surface, complicating approval for use in sensitive applications like diagnostics or clinical trial materials. I’ve consulted colleagues who straightforwardly rejected suppliers that couldn’t provide an unbroken chain of quality analysis, even as supply chains stretched thin in peak demand periods.
Solving these challenges starts with clear communication between producers and buyers. Regulatory frameworks have moved steadily towards higher transparency, requiring posted certificates of analysis, trace impurity data, and even third-party confirmation for sensitive applications. Reputable suppliers have responded by creating systems for batch tracking and customer audit access. Labs benefit from selecting vendors who can routinely provide documentation and respond quickly to queries about production practices or sourcing methods.
Expanded training for safe handling and the inclusion of neutralization kits in chemical stocks assist both teaching and research labs in dealing with the small, but real, risks posed by strong acids. Having procedures that stress quick reporting of errors or supply fluctuations keeps user groups—especially those in less-connected regions—in the loop before critical experiments grind to a halt.
Innovation around synthesis stands out as a long-term goal. Further development of low-solvent routes, recycling of spent process liquids, and bio-based alternatives for pyridine feedstocks offer hope for even lower environmental impact. Industry groups and universities have begun collaborating on shared best practices, publication of new methods, and open reporting of incidents or improvements. Having recently participated in a working group on sustainable chemistry, I see how sharing case studies, practical tips, and real-world outcomes will do more to improve 2.6-pyridine carboxylic acid production than strict regulation alone.
A good chemical product proves its value in reliable outcomes and stress-free handling. 2.6-pyridine carboxylic acid doesn't just fill an order sheet. It meets the needs of professionals who demand purity, reproducibility, and honest information about what goes into their research, analysis, teaching, or production. Real progress in science and industry grows on the back of these steady, trustworthy ingredients. With clear eyes on quality and sustainability, its path ahead looks promising.